Aussel C
Res Commun Chem Pathol Pharmacol. 1984 Jul;45(1):157-60.
The conversion of exogenous arachidonic acid into prostaglandin E2 (PGE2) was studied in human placenta and fetal membranes microsomes Rat and human alpha-fetoproteins (AFPs) at 170 micrograms/ml in the incubation medium, a concentration that does not exceed the physiological concentration observed in rat and human body fluids during pregnancy, decreased by 75% and 90% respectively the amount of PGE2 synthesized. The regulation of PGs synthesis by AFPs can shed a new light on different aspects of the numerous physiological actions of AFPs previously described such as ovarian regulation of immunosuppressive activity.
研究了人胎盘和胎膜微粒体中外源性花生四烯酸向前列腺素E2(PGE2)的转化。在孵育培养基中浓度为170微克/毫升的大鼠和人甲胎蛋白(AFP),该浓度不超过妊娠期间大鼠和人体体液中观察到的生理浓度,分别使合成的PGE2量减少了75%和90%。AFP对前列腺素合成的调节可以为先前描述的AFP众多生理作用的不同方面提供新的线索,例如卵巢对免疫抑制活性的调节。